Micronucleus counts correlating with male infertility: a clinical analysis of chromosomal abnormalities and reproductive parameters.

Shun-Han Zhang, Ying-Jun Xie, Wen-Jun Qiu, Qian-Ying Pan, Li-Hao Chen, Jian-Feng Wu, Si-Qi Huang, Ding Wang, Xiao-Fang Sun
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Abstract

Abstract: Investigating the correlation between micronucleus formation and male infertility has the potential to improve clinical diagnosis and deepen our understanding of pathological progression. Our study enrolled 2252 male patients whose semen was analyzed from March 2023 to July 2023. Their clinical data, including semen parameters and age, were also collected. Genetic analysis was used to determine whether the sex chromosome involved in male infertility was abnormal (including the increase, deletion, and translocation of the X and Y chromosomes), and subsequent semen analysis was conducted for clinical grouping purposes. The participants were categorized into five groups: normozoospermia, asthenozoospermia, oligozoospermia, oligoasthenozoospermia, and azoospermia. Patients were randomly selected for further study; 41 patients with normozoospermia were included in the control group and 117 patients with non-normozoospermia were included in the study group according to the proportions of all enrolled patients. Cytokinesis-block micronucleus (CBMN) screening was conducted through peripheral blood. Statistical analysis was used to determine the differences in micronuclei (MNi) among the groups and the relationships between MNi and clinical data. There was a significant increase in MNi in infertile men, including those with azoospermia, compared with normozoospermic patients, but there was no significant difference between the genetic and nongenetic groups in azoospermic men. The presence of MNi was associated with sperm concentration, progressive sperm motility, immotile spermatozoa, malformed spermatozoa, total sperm count, and total sperm motility. This study underscores the potential utility of MNi as a diagnostic tool and highlights the need for further research to elucidate the underlying mechanisms of male infertility.

与男性不育相关的微核计数:染色体异常和生殖参数的临床分析。
摘要:探讨微核形成与男性不育症的相关性,有助于提高临床诊断水平,加深对病理进展的理解。我们的研究招募了2252名男性患者,分析了他们在2023年3月至2023年7月期间的精液。他们的临床资料,包括精液参数和年龄也被收集。通过遗传分析确定与男性不育相关的性染色体是否异常(包括X、Y染色体的增加、缺失、易位),随后进行精液分析进行临床分型。参与者被分为五组:无精子症、弱精子症、少精子症、少精子症和无精子症。随机选择患者进行进一步研究;将41例正常精子症患者纳入对照组,117例非正常精子症患者按入组患者比例纳入研究组。通过外周血进行细胞分裂阻断微核(cmbn)筛选。统计学分析各组间微核(MNi)的差异及与临床资料的关系。与正常精子患者相比,包括无精子症患者在内的不育男性的MNi显著增加,但无精子症男性的遗传组与非遗传组之间无显著差异。MNi的存在与精子浓度、进行性精子活力、不动精子、畸形精子、总精子数和总精子活力有关。这项研究强调了MNi作为诊断工具的潜在效用,并强调了进一步研究以阐明男性不育的潜在机制的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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